@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_head
{
this:
np:hasAssertion
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_assertion
;
np:hasProvenance
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_provenance
;
np:hasPublicationInfo
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_assertion
a
np:Assertion
.
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_provenance
a
np:Provenance
.
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_assertion
{
miriam-gene:1371
a
ncit:C16612
.
lld:C0036690
a
ncit:C7057
.
dgn-gda:DGNad3cc1f05eed0dce1d8c7cabf48861a1
sio:SIO_000628
miriam-gene:1371
,
lld:C0036690
;
a
sio:SIO_001121
.
}
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_provenance
{
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_assertion
dcterms:description
"[Given that COX catalytic subunits are encoded by mtDNA, the objective of the present study was to explore whether mtDNA population genetic variation could affect COX activity and quantity and favors sepsis survival.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:22251664
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP768150.RAxJcJHLGgPeTxSC4N23gpu9P50-TxPkNqztW5LsUHzmM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}